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Computational analysis of human medium-chain dehydrogenases/reductases revealing substrate- and coenzyme-binding characteristics

Chemico-biological interactions, 2024-02, Vol.390, p.110876-110876, Article 110876

2024

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In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

Clinical endocrinology (Oxford), 2015-01, Vol.82 (1), p.37-44

2015

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Alcohol dehydrogenase, SDR and MDR structural stages, present update and altered era

Chemico-biological interactions, 2015-06, Vol.234, p.75-79

2015

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Computational studies of human class V alcohol dehydrogenase - the odd sibling

BMC biochemistry, 2016-07, Vol.17 (1), p.16-16, Article 16

2016

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Mammalian alcohol dehydrogenases – A comparative investigation at gene and protein levels

Chemico-biological interactions, 2011-05, Vol.191 (1), p.2-7

2011

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A subdivided molecular architecture with separate features and stepwise emergence among proinsulin C-peptides

Biochemical and biophysical research communications, 2014-08, Vol.450 (4), p.1433-1438

2014

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Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

Clinical biochemistry, 2019-11, Vol.73, p.50-56

2019

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The mammalian alcohol dehydrogenase genome shows several gene duplications and gene losses resulting in a large set of different enzymes including pseudoenzymes

Chemico-biological interactions, 2015-06, Vol.234, p.80-84

2015

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Analysis of mammalian alcohol dehydrogenase 5 (ADH5): Characterisation of rat ADH5 with comparisons to the corresponding human variant

Chemico-biological interactions, 2013-02, Vol.202 (1-3), p.97-103

2013

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Enrichment of ligands with molecular dockings and subsequent characterization for human alcohol dehydrogenase 3

Cellular and molecular life sciences : CMLS, 2010, Vol.67 (17), p.3005-3015

2010

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Transthyretin microheterogeneity and molecular interactions: implications for amyloid formation

Biomolecular concepts, 2014-06, Vol.5 (3), p.257-264

2014

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In vitro functional studies of rare CYP 21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

Clinical endocrinology (Oxford), 2015-01, Vol.82 (1), p.37-44

2015

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Computational Exploration of the Medium-Chain Dehydrogenase/Reductase Superfamily

Östberg, Linus J

2017

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Transthyretin microheterogeneity and molecular interactions: implications for amyloid formation

Biomolecular concepts, 2014-06, Vol.5 (3), p.257

2014

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Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects

International Journal of Endocrinology, 2016-01, Vol.2016 (2016), p.509-518-057

2016

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Computational analysis of human medium-chain dehydrogenases/reductases revealing substrate- and coenzyme-binding characteristics

In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

Alcohol dehydrogenase, SDR and MDR structural stages, present update and altered era

Computational studies of human class V alcohol dehydrogenase - the odd sibling

Mammalian alcohol dehydrogenases – A comparative investigation at gene and protein levels

A subdivided molecular architecture with separate features and stepwise emergence among proinsulin C-peptides

Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

The mammalian alcohol dehydrogenase genome shows several gene duplications and gene losses resulting in a large set of different enzymes including pseudoenzymes

Analysis of mammalian alcohol dehydrogenase 5 (ADH5): Characterisation of rat ADH5 with comparisons to the corresponding human variant

Enrichment of ligands with molecular dockings and subsequent characterization for human alcohol dehydrogenase 3

Transthyretin microheterogeneity and molecular interactions: implications for amyloid formation

In vitro functional studies of rare CYP 21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

Computational Exploration of the Medium-Chain Dehydrogenase/Reductase Superfamily

Transthyretin microheterogeneity and molecular interactions: implications for amyloid formation

Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects

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